Italian National Registry of Alopecia Areata: An Epidemiological Study of 699 Italian Patients

    Bianca Maria Piraccini, Luca Rapparini, Federico Quadrelli, Aurora Alessandrini, Francesca Bruni, Stephano Cedirian, Francesca Pampaloni, Emanuela Marcelli, Barbara Bortolani, Enrico Giampieri, Giuseppe Gallo, Francesca Torrelli, Nadia Sciamarrelli, Pietro Quaglino, Carlo Tomasini, Stefania Barruscotti, Francesca Ambrogio, Caterina Foti, Michele Picciallo, Gemma Caro, Alfredo Rossi, Giovanni Pellacani, Lorenzo Ala, Maria Cristina Acri, Laura Diluvio, Enrico Matteini, Luca Bianchi, Giuseppe Argenziano, Graziella Babino, Elisabetta Fulgione, Laura Gnesotto, Andrea Sechi, Luigi Naldi, F. Tassone, Ketty Peris, Giacomo Caldarola, Raffaele Dante Caposiena, Giulia Bazzacco, Iris Zalaudek, Maria Giovanna Vastarella, Mariateresa Cantelli, Angela Patrì, Federica Dall’Oglio, Francesco Lacarrubba, Giuseppe Micali, Alessandro Fraghì, Valeria Boccaletti, Angelo Valerio Marzano, Mauro Barbareschi, Martina Silvio, Emanuele Vagnozzi, Maria Concetta Fargnoli, Chiara Caponio, Laura Atzori, Silvia Sanna, Jasmine Anedda, Claudio Feliciani, Maria Beatrice De Felici Del Giudice, Ilaria Scandagli, Francesca Prignano, Franco Rongioletti, Antonio Podo Brunetti, Gianmarco D Bigotto, Anna Maria Offidani, Oriana Simonetti, Serena Lembo, Annunziata Raimondo, Riccardo Balestri, Tommaso Ioris, Paolo Gisondi, Francesco Bellinato, Emanuele Trovato, Élisa Cinotti, Manuela Papini, Michela Cicoletti, Monica Corazza, Michela Starace
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    Studysummary This study supports the use of a national registry as an effective tool for documenting epidemiological data, disease progression, treatment responses, and quality of life impacts in patients with alopecia areata.
    Automatically generated from the study's abstract, not written by a person, and not a review of the full paper. Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer
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